Canonical Allele Identifier: PA1139737337
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 873986
ClinVar RCV Id: RCV001096582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His1898Leu
CA344024756
NM_018136.5:c.5693A>T